Episode 301 - Hall Skåra episode artwork

EPISODE · Nov 21, 2019 · 5 MIN

Episode 301 - Hall Skåra

from I'm Aware That I'm Rare: the phaware® podcast · host phaware global association

Hall Skåra is a pulmonary hypertension patient from Norway. He became part of PHA Europe's staff after his diagnosis. He has helped develop their "White Spots" program, which establishes new PH patient associations in countries where they don't exist. In this episode, Hall discusses the first ever PAH Patient Charter that was launched on November 12, 2019 to coincide with PH Awareness Month. The Charter was facilitated and sponsored by Actelion, a Janssen Pharmaceutical Company of Johnson & Johnson and a PAH-expert Steering Committee made up of patients, patient advocates and healthcare professionals. #PAHPatientCharter #phawarenessmonth  Learn more about pulmonary hypertension trials at www.phaware.global/clinicaltrials. Never miss an episode with the phaware® podcast app. Follow us @phaware on Facebook, Twitter, Instagram, YouTube & Linkedin Engage for a cure: www.phaware.global/donate #phaware #ClinicalTrials  @actelion_com @EuropePHA @PHAssociation @wginsing @PhDeutschland @LatinosConHP @Hellenic_PH @phsingapore

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Episode 301 - Hall Skåra

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This episode is 5 minutes long.

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This episode was published on November 21, 2019.

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Hall Skåra is a pulmonary hypertension patient from Norway. He became part of PHA Europe's staff after his diagnosis. He has helped develop their "White Spots" program, which establishes new PH patient associations in countries where they don't...

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